Emory Clinic
Atlanta, Georgia, 30322, United States
NCT Number: NCT04005495
The aim of the project is to evaluate the feasibility and acceptance of a teaching kitchen program as a worksite wellness program at Emory University
Looking for future studies?
Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Atlanta, Georgia, 30322, United States
The teaching kitchen model is an innovative, multidisciplinary approach for motivating and establishing healthful habits and behaviors. The self-care program combines didactic information with experiential learning in nutrition, culinary arts, exercise, yoga, and mindfulness. The aim of the project is to evaluate the feasibility and acceptance of teaching kitchen program as a worksite wellness program at Emory University. Changes in biomarkers and self-reported behaviors will be evaluated up to one year.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The teaching kitchen program will include five 4-hour Saturday classes every other weekend over the course of 10 weeks (5 sessions totaling 20 hours of instruction). It will be taught by subject matter experts from the Emory University faculty and staff as well as potentially from the community. The classes will include the scientific rationale, practical applications, and recommendations for implementing self-care components into participants' daily lives. Experiential learning will include hands-on cooking demonstrations, mindfulness-based lunches, a yoga session, and a group exercise session. Rather than being prescriptive, the lectures and demonstrations are geared to inspire self-designed and personalized alterations in dietary patterns and behaviors that will match participants' culture, preferences, and health conditions. Biometrics and survey instruments will be assessed at 4 times: at baseline, after the 10-week program, and at 6 and 12 months after the program.
Time frame: 2-week visit
Program attendance will be assessed by calculating percent of enrolled participants completing the program visits
Time frame: 4-week visit
Program attendance will be assessed by calculating percent of enrolled participants completing the program visits
Time frame: 6-week visits
Program attendance will be assessed by calculating percent of enrolled participants completing the program visits
Time frame: 8-week visit
Program attendance will be assessed by calculating percent of enrolled participants completing the program visits
Time frame: 10-week visit
Program completion will be assessed by calculating percent of participants completing the program
Time frame: Baseline, 10-week, and 6 and 12 months after the program
RAND Health 36-Item scale is used to evaluate global health, quality of life, and presenteeism. All items are scored so that a high score defines a more favorable health state. In addition, each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively. Scores represent the percentage of total possible score achieved.
Time frame: Baseline, 10-week, and 6 and 12 months after the program
A single question will be asked about the frequency of absence from work
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Body composition will be measured by seca medical Body Composition Analyzer (mBCA) 515. This device utilizes 8-point Bioelectrical Impedance Analysis to assess percent body fat. This is a non-invasive technique, taking about two minutes, that requires standing on a scale.
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Body Mass Index (BMI) is a person's weight in kilograms divided by the square of height in meters.
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Blood pressure will be measured using blood pressure monitor
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Blood pressure will be measured using blood pressure monitor
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Dietary Intake will be assessed using the 8-item Starting The Conversation brief dietary assessment and intervention tool for health professionals. Response options for the survey items are organized into three columns: the left column indicates the most healthful dietary practices (scored 0); the center column indicates less healthful practices (scored 1); and the right column indicates the least healthful practices (scored 2). Item scores are added to create a summary score (range 0-16), with lower summary scores reflecting a more healthful diet and higher scores reflecting the greatest room for improvement.
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Cooking Frequency and Confidence questionnaire - items 1,2, 8- will be used to assess change in habits pre to post intervention.Responses range on a scale of 1-6. Higher score reflects more favorable state and lower score reflects the greatest room for improvement.
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Cooking Frequency and Confidence questionnaire will be used to assess confidence to prepare new recipes from basic ingredients. Items 3-7 (assessing cooking confidence) are scored on a scale of 0-10 in a summative fashion. Higher summary score reflects more favorable state and lower summary score reflects the greatest room for improvement.
Time frame: Baseline, 10-week, and 6 and 12 months after the program
The brief Physical Activity "Vital Sign" (PAVS) will be used to determine if participants achieve the recommended amount of physical activity, with an additional question to assess use of yoga.Two questions are self-reported: 1) "How many days during the past week have you performed physical activity where your heart beats faster and your breathing is harder than normal for 30 minutes or more?" and 2) "How many days in a typical week do you perform activity such as this?" The responses are reported as days during the past week over days in a typical week, with scores ranging from 0 to 7 for each question. PAVS requires less than 30 seconds to administer and score
Time frame: Baseline, 10-week, and 6 and 12 months after the program
The PSS-10 is a self-report instrument consisting of 10 items purported to assess "how unpredictable, uncontrollable, and overloaded respondents find their lives". Each of the items on the PSS-10 are rated on a 5-point Likert scale, ranging from 0 (never) to 4 (very often). The PSS-10 consisted of 6 positively (items 1, 2, 3, 6, 9 and 10: Positive factor) and 4 negatively (items 4, 5, 7 and 8: Negative factor) worded items. Negative worded items were re-coded during analysis. Total scores range from 0 to 40, with higher scores indicating higher levels of perceived stress
Time frame: Baseline, 10-week, and 6 and 12 months after the program
Mindful eating practices will be assessed using this Mindfulness and Mindful Eating tool. Domains of the 28-item questionnaire are: Disinhibition, Awareness, External Cues, Emotional Response, and Distraction. For all items, response options are "Never/Rarely," "Sometimes," "Often," and "Usually/Always". Each item is scored from 1 to 4, where higher scores signified more mindful eating. Each subscale score is calculated as the mean of items. The summary score is the mean of the 5 subscales.
Emory University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07227220
Behavior, Behavior, Health
Houston, Texas, United States
View Trial DetailsNCT06383481
Endocrine System Diseases, Healthy Lifestyle
Erzurum, palandöken, Turkey (Türkiye)
View Trial DetailsNCT04802291
Behavior, Body Weight
New Brunswick, New Jersey, United States
View Trial DetailsNCT05678426
Behavior, Fasting
Hall in Tirol, Tyrol, Austria
View Trial Details